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rs61760925

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61760925(C;T)
Make rs61760925(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944386
GeneHLA-A
is asnp
is mentioned by
dbSNPrs61760925
ebirs61760925
HLIrs61760925
Exacrs61760925
Varsomers61760925
Maprs61760925
PheGenIrs61760925
hapmaprs61760925
1000 genomesrs61760925
hgdprs61760925
ensemblrs61760925
gopubmedrs61760925
geneviewrs61760925
scholarrs61760925
googlers61760925
pharmgkbrs61760925
gwascentralrs61760925
openSNPrs61760925
23andMers61760925
23andMe allrs61760925
SNP Nexus

SNPshotrs61760925
SNPdbers61760925
MSV3drs61760925
GWAS Ctlgrs61760925
Max Magnitude0
ClinVar
Risk rs61760925(G,T;G,T)
Alt rs61760925(G,T;G,T)
Reference rs61760925(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912163C>G; NC_000006.11:g.29912163C>T
CLNSRC
CLNACC